Powers On
YesCosmetic
GoodCosmetic Condition
New in box
Excellent
Good
Poor
Overview
Description:
The 3M ESPE RotoMix Dental Capsule Mixing Unit, Model D82229, is a laboratory and dental equipment mixing device designed for use with compatible dental material capsules. Its mixing mechanism provides a consistent mixing process for capsule-based materials, supporting preparation workflows in dental laboratory and clinical environments. The compact unit is designed for countertop placement and operates on a 120V electrical input at 60Hz, making it suitable for compatible dental equipment setups.
Specifications:
Brand: 3M
Model: D82229
Product Name: RotoMix
Product Type: Dental Capsule Mixing Unit
Equipment Type: Dental Mixing Equipment
Mixing Type: Capsule Mixing
Voltage: 120V
Frequency: 60Hz
Function: Dental Material Mixing
Application: Dental Laboratory / Dental Practice
Features:
RotoMix capsule mixing configuration
Designed for compatible dental material capsules
Automated mixing operation
Compact countertop design
120V electrical input
60Hz frequency compatibility
Suitable for dental material preparation workflows
Technical Details
| Brand | 3M |
|---|---|
| Category | Dental Capsule Mixing Unit |
| Medical Discipline | General Surgery |
| Condition | Used |
| Cosmetic Condition | Good |
| Powers On | Yes |
| OEM | 3M |
| SKU | DA433-ITEM-EE |
| Warranty | 30 - Warranty |
Need This Product Certified Patient-Ready?
If you require this product to be patient-ready certified, you can request a quote. Inspection, testing, repair, electrical safety testing, and calibration services are available through A Biomedical Service, Inc.
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No similar items available.
Safety & Biomedical Inspection Notice
Shipping & Receiving Notice
Medical equipment may require inspection, functional verification, calibration, preventive maintenance, safety testing, or other evaluations following transportation and before being placed into service.
Upon receipt, the purchaser is responsible for inspecting the equipment for any shipping damage and determining whether any inspection, testing, calibration, preventive maintenance, or certification is necessary based on the manufacturer's recommendations, the receiving facility's policies, and all applicable laws and regulations.
The equipment should not be placed into clinical service or used for patient care until the purchaser has verified that it is safe, appropriate, and compliant for its intended use.
Biomedical Inspection Notice
Medical equipment should be evaluated by qualified personnel before being placed into clinical service. Depending on the type of equipment, the evaluation may include, as applicable:
- Electrical safety testing
- Functional performance verification
- Alarm verification (if applicable)
- Battery inspection or replacement (if applicable)
- Calibration verification (if applicable)
- Preventive maintenance
- Software configuration and system settings
- Verification of compatible accessories, consumables, and disposables
- Inspection for shipping or handling damage
- Compliance with the manufacturer's recommendations
- Compliance with the receiving facility's policies, procedures, and applicable regulatory requirements
Transportation, storage, handling, and installation may affect the performance of medical equipment. Reuse Medical recommends that the receiving facility inspect, test, and evaluate the equipment in accordance with the manufacturer's recommendations and the facility's biomedical engineering procedures before placing the equipment into clinical service or patient use.
